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Pediatric pyoderma gangrenosum: is it just big wounds on little adults?
Tahereh Soleimani1, Sarah E Sasor2, Leigh Spera3
1Department of Surgery, College of Human Medicine, Michigan State University, East Lansing, Michigan.
Insights
Pediatric pyoderma gangrenosum (PG) is more strongly linked to gastrointestinal, rheumatologic, and vascular conditions than adult PG. This finding suggests a different diagnostic approach is needed for children with this rare skin condition.
Area of Science:
- Dermatology
- Pediatrics
- Epidemiology
Background:
- Pyoderma gangrenosum (PG) is a rare ulcerative skin condition.
- It can be misdiagnosed as a bacterial infection requiring surgery.
- Prompt medical treatment is crucial to prevent severe complications.
Purpose of the Study:
- To investigate if pediatric PG has different associated conditions compared to adult PG.
- To determine if a different medical workup is necessary for children with PG.
Main Methods:
- Utilized the National Inpatient Sample and Kids' Inpatient Database.
- Identified hospitalized PG patients using ICD-9 codes.
- Compared PG patients with non-PG patients, analyzing associated diagnoses.
Main Results:
- Adult and pediatric PG patients were more likely to be female and have arteritis, arthropathy, and colitis.
- Pediatric PG showed a significantly higher association with arteritis, arthropathy, and colitis compared to adults.
- Pediatric PG was less associated with malignancy than adult PG.
Conclusions:
- This study is the largest to compare adult and pediatric PG.
- Pediatric PG is more associated with gastrointestinal, rheumatologic, and vascular issues.
- The distinct associations in children necessitate a tailored diagnostic approach for pediatric PG.
Background:
Pyoderma gangrenosum (PG) is an uncommon, ulcerative, cutaneous condition, often caused by surgical trauma that can masquerade as a pyogenic disease process requiring debridement and antibiotics. Treatment is, however, medical, with delay leading to significant morbidity. In addition, medical workup for coincident disorders has been suggested. The purpose of this study was to test the hypothesis that pediatric PG has differing disease associations and therefore requires a differing medical workup.
Methods:
The National Inpatient Sample and the Kids' Inpatient Database were used to identify all hospitalized patients with PG. PG patients were identified using International Classification of Diseases-9 code and divided into adults and children. For each age group, the PG patients were compared with non-PG patients. The Breslow-Day test was used to determine the relationship between PG and associated diagnoses.
Results:
There were 204 of 7,384,591 children and 10,154 of 89,674,318 adults with PG. Both adult and pediatric PG patients were more likely to be female and have arteritis, arthropathy, and colitis. The PG children had a significantly greater odds ratio for having arteritis, arthropathy, and colitis but not malignancy when compared to adults.
Conclusions:
This is the largest study of PG in adult and child populations. It validates the associations known regarding adult PG while demonstrating that pediatric PG is much more highly associated with gastroenterologic, rheumatologic, and vascular issues and less likely to be coincident with malignancy. These differences demonstrate a need to approach the disease differently in the pediatric population, with regard to associated diagnosis.
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